Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)
Multiplex Assay Kit for Procollagen I N-Terminal Propeptide (PINP) ,etc. by FLIA (Flow Luminescence Immunoassay)
P1NP; N-Propeptide Of Type I Procollagen; Procollagen I Amino Terminal Propeptide
（注：單次混測多因子不超過8個(gè)指標(biāo) ）
- 編號(hào)ULMA957Ra
- 物種Rattus norvegicus (Rat，大鼠) 相同的名稱，不同的物種。
- 實(shí)驗(yàn)方法競爭抑制
- 反應(yīng)時(shí)長1.5h
- 檢測范圍19.53-20000pg/mL
- 靈敏度最小可檢測劑量小于等于6.51 pg/mL.
- 樣本類型Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
- 下載 英文說明書 中文說明書
- 規(guī)格 8指標(biāo)數(shù) 7指標(biāo)數(shù) 6指標(biāo)數(shù) 5指標(biāo)數(shù) 4指標(biāo)數(shù) 3指標(biāo)數(shù) 2指標(biāo)數(shù)1指標(biāo)數(shù)
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通過ISO 9001、ISO 13485質(zhì)量體系認(rèn)證
特異性
本試劑盒用于檢測Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)，經(jīng)檢測與其它相似物質(zhì)無明顯交叉反應(yīng)。
由于受到技術(shù)及樣本來源的限制，不可能完成對(duì)所有相關(guān)或相似物質(zhì)交叉反應(yīng)檢測，因此本試劑盒有可能與未經(jīng)檢測的其它物質(zhì)有交叉反應(yīng)。
回收率
分別于定值血清及血漿樣本中加入一定量的Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)（加標(biāo)樣品），重復(fù)測定并計(jì)算其均值，回收率為測定值與理論值的比率。
| 樣本 | 回收率范圍(%) | 平均回收率(%) |
| serum(n=5) | 81-101 | 96 |
| EDTA plasma(n=5) | 80-104 | 90 |
| heparin plasma(n=5) | 92-105 | 97 |
| sodium citrate plasma(n=5) | 87-95 | 92 |
精密度
精密度用樣品測定值的變異系數(shù)CV表示。CV(%) = SD/mean×100
批內(nèi)差：取同批次試劑盒對(duì)低、中、高值定值樣本進(jìn)行定量檢測,每份樣本連續(xù)測定20 次，分別計(jì)算不同濃度樣本的平均值及SD值。
批間差：選取3個(gè)不同批次的試劑盒分別對(duì)低、中、高值定值樣本進(jìn)行定量測定，每個(gè)樣本使用同一試劑盒重復(fù)測定8次，分別計(jì)算不同濃度樣本的平均值及SD值。
批內(nèi)差： CV<10%
批間差： CV<12%
線性
在定值血清及血漿樣本內(nèi)加入適量的Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)，并倍比稀釋成1:2，1:4，1:8，1:16的待測樣本，線性范圍即為稀釋后樣本中Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)含量的測定值與理論值的比率。
| 樣本 | 1:2 | 1:4 | 1:8 | 1:16 |
| serum(n=5) | 90-104% | 89-96% | 88-95% | 78-101% |
| EDTA plasma(n=5) | 83-90% | 80-97% | 94-101% | 83-101% |
| heparin plasma(n=5) | 78-93% | 88-96% | 98-105% | 89-103% |
| sodium citrate plasma(n=5) | 94-102% | 92-101% | 80-94% | 85-99% |
穩(wěn)定性
經(jīng)測定，試劑盒在有效期內(nèi)按推薦溫度保存，其活性降低率小于5%。
為減小外部因素對(duì)試劑盒破壞前后檢測值的影響，實(shí)驗(yàn)室的環(huán)境條件需盡量保持一致，尤其是實(shí)驗(yàn)室內(nèi)溫度、濕度及溫育條件。其次由同一實(shí)驗(yàn)員來進(jìn)行操作可減少人為誤差。
實(shí)驗(yàn)流程
1. 實(shí)驗(yàn)前標(biāo)準(zhǔn)品、試劑及樣本準(zhǔn)備；
2. 加樣（標(biāo)準(zhǔn)品、樣本、磁珠、檢測溶液A）標(biāo)準(zhǔn)品或樣本50μL及磁珠10μL，加檢測溶液A50μL，
37°C酶標(biāo)板振蕩器孵育60分鐘；
3. 磁吸洗板3次；
4. 加檢測溶液B100μL，37°C振動(dòng)孵育30分鐘；
5. 磁吸洗板3次；
6. 加鞘液100μL，旋渦震蕩2分鐘后讀數(shù)。
實(shí)驗(yàn)原理
將Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)抗體包被于磁珠，制成固相載體，向微孔中分別加入標(biāo)準(zhǔn)品或標(biāo)本以及磁珠、標(biāo)記VEGFA，標(biāo)記的Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)和未標(biāo)記的Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)與連接于固相載體上的抗體競爭結(jié)合，然后將未結(jié)合物洗凈后，加入PE標(biāo)記的親和素，再次徹底洗滌后即可上機(jī)讀數(shù)。MFI值和樣品中的Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法)呈負(fù)相關(guān)。
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| 編號(hào) | 適用物種：Rattus norvegicus (Rat，大鼠) | 應(yīng)用(僅供研究使用，不用于臨床診斷！) |
| URPA957Ra01 | Ⅰ型前膠原氨基端原肽(PINP)重組蛋白 | Positive Control; Immunogen; SDS-PAGE; WB. |
| UAPA957Ra01 | Ⅰ型前膠原氨基端原肽(PINP)活性蛋白 | Cell?culture;?Activity?Assays. |
| UCPA957Ra21 | Ⅰ型前膠原氨基端原肽(PINP)卵白蛋白偶聯(lián)物 | Immunogen; SDS-PAGE; WB. |
| UPAA957Ra01 | Ⅰ型前膠原氨基端原肽(PINP)多克隆抗體 | WB; IHC |
| ULAA957Ra71 | Ⅰ型前膠原氨基端原肽(PINP)多克隆抗體(生物素標(biāo)記) | WB; IHC; ICC. |
| USEA957Ra | Ⅰ型前膠原氨基端原肽(PINP)檢測試劑盒(酶聯(lián)免疫吸附試驗(yàn)法) | Enzyme-linked immunosorbent assay for Antigen Detection. |
| UIEA957Ra | Ⅰ型前膠原氨基端原肽(PINP)檢測試劑盒(酶聯(lián)免疫吸附試驗(yàn)法,快捷型) | Enzyme-linked immunosorbent assay for Antigen Detection. |
| UCEA957Ra | Ⅰ型前膠原氨基端原肽(PINP)檢測試劑盒(酶聯(lián)免疫吸附試驗(yàn)法) | Enzyme-linked immunosorbent assay for Antigen Detection. |
| ULMA957Ra | Ⅰ型前膠原氨基端原肽(PINP)等多因子檢測試劑盒(流式熒光發(fā)光法) | FLIA Kit for Antigen Detection. |
| UKSA957Ra11 | Ⅰ型前膠原氨基端原肽(PINP)檢測試劑盒DIY材料(酶聯(lián)免疫吸附試驗(yàn)法) | Main materials for "Do It (ELISA Kit) Yourself". |
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